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Old 02-16-2007, 03:52 PM
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reverett123 reverett123 is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default Darn, ZF, that one's going to take some getting used to

Very perturbing. (Hey, there's a PD motto for you!)

What are we to make of this? Lewy Bodies show up there first, but against all common sense the neuronal density is doubled? And I still can't smell? So...
1) Could it be that the extra neurons are some sort of attempt to compensate or something?
2) Whatever it is, is there some way that the effect could be triggered in the SN? Or is it a genetic feature?

I'm never bored. -Rick



Quote:
Originally Posted by ZucchiniFlower View Post
This is interesting. Too many dopaminergic cells in the olfactory bulb cause loss of smell....


Movement Disorders

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Volume 19, Issue 6 , Pages 687 - 692

Published Online: 8 Jan 2004

Brief Report
A 100% increase of dopaminergic cells in the olfactory bulb may explain hyposmia in Parkinson's disease
Evelien Huisman, BSc 1 *, Harry B.M. Uylings, PhD 1 2, Piet V. Hoogland, MD, PhD 1 3

Abstract
Hyposmia is one of the most prevalent symptoms of Parkinson's disease. It may occur even before the motor symptoms start. To determine whether the olfactory dysfunctions, like the motor symptoms, are associated with a loss of dopamine, the number of dopaminergic cells in the olfactory bulb of Parkinson's disease patients was studied using tyrosine hydroxylase immunohistochemistry.

The quantitative analysis reveals that the total number of tyrosine hydroxylase-immunoreactive neurons in the olfactory bulb is twice as high in Parkinson patients compared to age and gender-matched controls. Because dopamine is known to inhibit olfactory transmission in the olfactory glomeruli, we suggest that the increase of dopaminergic neurons in the olfactory bulb is responsible for the hyposmia in Parkinson patients.

The increase of dopamine in the olfactory bulb explains why olfaction does not improve with levodopa therapy.

http://www3.interscience.wiley.com/c...9783/HTMLSTART
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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